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rs1057519907

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519907(A;C)
Make rs1057519907(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54728057
GeneKIT
is asnp
is mentioned by
dbSNPrs1057519907
dbSNP (old)rs1057519907
ClinGenrs1057519907
ebirs1057519907
HLIrs1057519907
Exacrs1057519907
Gnomadrs1057519907
Varsomers1057519907
Maprs1057519907
PheGenIrs1057519907
Biobankrs1057519907
1000 genomesrs1057519907
hgdprs1057519907
ensemblrs1057519907
gopubmedrs1057519907
geneviewrs1057519907
scholarrs1057519907
googlers1057519907
pharmgkbrs1057519907
gwascentralrs1057519907
openSNPrs1057519907
23andMers1057519907
23andMe allrs1057519907
SNPshotrs1057519907
SNPdbers1057519907
MSV3drs1057519907
GWAS Ctlgrs1057519907
Max Magnitude0
ClinVar
Risk rs1057519907(C;C)
Alt rs1057519907(C;C)
Reference Rs1057519907(A;A)
Significance Probable-Pathogenic
Disease Malignant melanoma of skin Adenocarcinoma of stomach
Variation info
Gene KIT
CLNDBN Malignant melanoma of skin Adenocarcinoma of stomach
Reversed 0
HGVS NC_000004.11:g.55594223A>C
CLNSRC
CLNACC RCV000428962.1, RCV000439220.1,